Cleared Traditional

K060900 - SPACELABS MEDICAL BISPECTRAL INDEX (BISX) ANALYSIS MODULE 91482 AND ACCESSORIES MODEL-91842

K060900 is an FDA 510(k) clearance for SPACELABS MEDICAL BISPECTRAL INDEX (BIS..., manufactured by Spacelabs Medical, Inc.. The device is a Class 2 Neurology device with product code OLW cleared through the Traditional 510(k) pathway after a 81-day FDA review.

K060900 · Spacelabs Medical, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2006
Decision
81d
Days
Class 2
Risk

K060900 is an FDA 510(k) clearance for the SPACELABS MEDICAL BISPECTRAL INDEX (BISX) ANALYSIS MODULE 91482 AND ACCESSORI.... Classified as Index-generating Electroencephalograph Software (product code OLW), Class II - Special Controls.

Submitted by Spacelabs Medical, Inc. (Issaquah, US). The FDA issued a Cleared decision on June 23, 2006 after a review of 81 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1400 - the FDA neurology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Spacelabs Medical, Inc. devices

FDA 510(k) Submission Details - K060900

510(k) Number K060900 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 2006
Decision Date June 23, 2006
Days to Decision 81 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 149d · This submission: 81d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OLW Device Classification - Class 2, Special Controls

Product Code OLW Index-generating Electroencephalograph Software
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1400
Definition Analyze Electrical Activity Of The Brain By Transformation Of Electroencephalograph Signals Into A Dimensionless Index Number For Use And Interpretation By A Qualified User.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Neurology devices follow this clearance model.

Regulatory Peers - OLW Index-generating Electroencephalograph Software

All 38
Devices cleared under the same product code (OLW) and FDA review panel - the closest regulatory comparables to K060900.
BIS EEG VISTA MONITOR SYSTEM AND BISX
K072286 · Aspect Medical Systems, Inc. · Nov 2007
BIS MODULE FOR ENVOY PATIENT MONITOR
K071899 · Mennen Medical , Ltd. · Oct 2007
BIS EEG MONITOR VIEW
K062613 · Aspect Medical Systems, Inc. · Jun 2007
SNAP II EEG MONITOR
K060997 · Everest Biomedical Instruments Co. · Jun 2006
BIS EEG MONITOR, MODEL BISX4
K052981 · Aspect Medical Systems, Inc. · Nov 2005
BIS EEG MONITOR, MODEL A-3000
K052362 · Aspect Medical Systems, Inc. · Sep 2005